Canonical Allele Identifier: CA2830536400

Gene: RAB28

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.13368856_13368857insG , CM000666.2:g.13368856_13368857insG	GRCh38
NC_000004.11:g.13370480_13370481insG , CM000666.1:g.13370480_13370481insG	GRCh37
NC_000004.10:g.12979578_12979579insG	NCBI36
NG_033891.1:g.120509_120510insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288723.9:c.*6-207_*6-206insC MANE Plus Clinical	ENSP00000288723.4:n.*6-207_*6-206insC
ENST00000330852.10:c.574-207_574-206insC MANE Select	ENSP00000328551.5:n.574-207_574-206insC
ENST00000288723.8:c.*6-207_*6-206insC	ENSP00000288723.4:n.*6-207_*6-206insC
ENST00000330852.9:c.574-207_574-206insC	ENSP00000328551.5:n.574-207_574-206insC
ENST00000338176.8:c.*32-207_*32-206insC	ENSP00000340079.4:n.*32-207_*32-206insC
ENST00000504644.1:c.256-207_256-206insC
ENST00000508274.5:c.*156-207_*156-206insC	ENSP00000424043.1:n.*156-207_*156-206insC
ENST00000511649.5:c.435+1014_435+1015insC
ENST00000630951.1:c.*251-207_*251-206insC	ENSP00000485808.1:n.*251-207_*251-206insC
NM_001017979.2:c.574-207_574-206insC	NP_001017979.1:n.574-207_574-206insC
NM_001159601.1:c.*32-207_*32-206insC	NP_001153073.1:n.*32-207_*32-206insC
NM_004249.3:c.*6-207_*6-206insC	NP_004240.2:n.*6-207_*6-206insC
XM_011513911.1:c.573+7688_573+7689insC	XP_011512213.1:n.573+7688_573+7689insC
XM_011513912.1:c.343-207_343-206insC	XP_011512214.1:n.343-207_343-206insC
XR_925360.1:n.789-7224_789-7223insC
XR_925361.1:n.788+7688_788+7689insC
NM_001017979.3:c.574-207_574-206insC MANE Select	NP_001017979.1:n.574-207_574-206insC
NM_004249.4:c.*6-207_*6-206insC MANE Plus Clinical	NP_004240.2:n.*6-207_*6-206insC
NM_001159601.2:c.*32-207_*32-206insC	NP_001153073.1:n.*32-207_*32-206insC